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Gene: LINC00323 (long intergenic non-protein coding RNA 323) Homo sapiens
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Symbol: LINC00323
Name: long intergenic non-protein coding RNA 323
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH aflatoxin B1; dioxygen; nickel atom
Type: ncrna
RefSeq Status: PREDICTED
Also known as: C21orf130; FLJ37173; NCRNA00323; PRED42
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2141,141,493 - 41,148,198 (-)EnsemblGRCh38hg38GRCh38
GRCh382141,141,500 - 41,148,064 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372142,513,427 - 42,524,877 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362142,513,427 - 42,519,991 (-)NCBINCBI36hg18NCBI36
Celera2127,711,607 - 27,718,170 (-)NCBI
Cytogenetic Map21q22.2NCBI
HuRef2127,982,332 - 27,988,895 (-)NCBIHuRef
CHM1_12142,073,760 - 42,080,323 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on LINC00323
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1603251
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.